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KMID : 0578320220450110855
Molecules and Cells
2022 Volume.45 No. 11 p.855 ~ p.867
CBP-Mediated Acetylation of Importin ¥á Mediates Calcium-Dependent Nucleocytoplasmic Transport of Selective Proteins in Drosophila Neurons
Cho Jae-Ho

Jo Min-Gu
Kim Eun-Seon
Lee Na-Yoon
Kim Soon-Ha
Chung Chang-Geon
Park Jeong-Hyang
Lee Sung-Bae
Abstract
For proper function of proteins, their subcellular localization needs to be monitored and regulated in response to the changes in cellular demands. In this regard, dysregulation in the nucleocytoplasmic transport (NCT) of proteins is closely associated with the pathogenesis of various neurodegenerative diseases. However, it remains unclear whether there exists an intrinsic regulatory pathway(s) that controls NCT of proteins either in a commonly shared manner or in a target-selectively different manner. To dissect between these possibilities, in the current study, we investigated the molecular mechanism regulating NCT of truncated ataxin-3 (ATXN3) proteins of which genetic mutation leads to a type of polyglutamine (polyQ) diseases, in comparison with that of TDP-43. In Drosophila dendritic arborization (da) neurons, we observed dynamic changes in the subcellular localization of truncated ATXN3 proteins between the nucleus and the cytosol during development. Moreover, ectopic neuronal toxicity was induced by truncated ATXN3 proteins upon their nuclear accumulation. Consistent with a previous study showing intracellular calcium-dependent NCT of TDP-43, NCT of ATXN3 was also regulated by intracellular calcium level and involves Importin ¥á3 (Imp ¥á3). Interestingly, NCT of ATXN3, but not TDP-43, was primarily mediated by CBP. We further showed that acetyltransferase activity of CBP is important for NCT of ATXN3, which may acetylate Imp ¥á3 to regulate NCT of ATXN3. These findings demonstrate that CBP-dependent acetylation of Imp ¥á3 is crucial for intracellular calcium-dependent NCT of ATXN3 proteins, different from that of TDP-43, in Drosophila neurons.
KEYWORD
ATXN3, CBP, Importin ¥á, acetylation, calcium, nucleocytoplasmic transport.
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